1. Home - LOVD - An Open Source DNA variation databaseLOVD stands for Leiden Open (source) Variation Database.LOVD's purpose : To provide a flexible, freely available tool for genomic variant and phenotype collection, display and curation. LOVD allows both patient-centered ...
2. LOVD - An Open Source DNA variation database.LOVD.NL Examples: DMD.lovd.nl, BRCA1.lovd.nl. See also our full list of LSDBs, or the list of registered LOVD installations.LOVD is supported by:LOVD is recommended by HVP and IRDiRC...
3. LOVD: easy creation of a locus-specific sequenceWe have developed the Leiden Open (source) Variation Database (LOVD) software approaching the "LSDB-in-a-Box" idea for the easy creation and maintenance of a fully web-based gene sequence variation database. LOVD is ...
4. User hlovdal - ServerhlovdalLinux user since 1994. 24 answers 0 questions ~163k people reached Norway serverfault.com/users/1223/… Member for 11 years, 11 months 61 profile views Last seen 2 days ago ...
5. Frontiers | Working-memory training in younger andSchmiedek, F., Lovden, M., and Lindenberger, U. (2010). Hundred days of cognitive training enhance broad cognitive abilities in adulthood: findings from the COGITO study.Front. Aging Neurosci. 2:27. doi: 10.3389/...
6. DCXR Gene - GeneCards | DCXR Protein | DCXRComplete information for DCXR gene (Protein Coding), Dicarbonyl And L-Xylulose Reductase, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium
7. The AAAS gene homepage - Global Variome sharedHomepage URL http://www.LOVD.nl/AAAS HGNC 13666 Entrez Gene 8086 PubMed articles AAAS OMIM - Gene 605378 OMIM - Diseases AAAS (achalasia-addisonianism-alacrimia syndrome (AAAS)) HGMD AAAS GeneCards AAAS GeneTest...
8. User hlovdal - Stackhlovdal Linux user since 1994. Main programming language: C. #SOreadytohelp (http://stackoverflow.com/10m) 635 answers 40 questions ~3.9m people reached Norway stackoverflow.com/users/23118/… Member for 12 yea...
9. Germline variation in BRCA1/2 is highly ethnic‐specific...Pathogenic 118 2 0.017 2 c.213‐12A?>?G BIC|BMD|LOVD|ClinVar|BED ‐ ‐ ‐ Pathogenic 257 4 0.016 16 c.5161C?>?T BMD|LOVD|ClinVar|BED|ENIGMA ‐ ‐ Stop gain ...
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